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Commission Decision of 13 April 2007 on the implementation of surveillance programmes for avian influenza in poultry and wild birds to be carried out in the Member States and amending Decision 2004/450/EC (notified under document number C(2007) 1554) (2007/268/EC) (repealed) in England

EU Decision 2007/268 · Adopted 3 May 2007 · Extends to United Kingdom

Original text. legislation.gov.uk does not revise this item, so later amendments are not shown here. Changes made to it are listed under each provision when known.

Commission Decision

of 13 April 2007

on the implementation of surveillance programmes for avian influenza in poultry and wild birds to be carried out in the Member States and amending Decision 2004/450/EC

(notified under document number C(2007) 1554)

(2007/268/EC) (repealed)

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Annotations to the whole text

Textual amendments

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Repealed by Commission Decision of 25 June 2010 on the implementation by Member States of surveillance programmes for avian influenza in poultry and wild birds (notified under document C(2010) 4190) (Text with EEA relevance) (2010/367/EU).

Contents

  1. 1Approval of surveillance programmes for avian influenza Repealed
  2. 2Amendments to Decision 2004/450/EC Repealed
  3. 3Article 3 Repealed
  4. Annex I: Guidelines on the implementation of surveillance programmes for avian influenza in poultry to be carried out in the Member States Repealed
  5. Objectives, general requirements and criteria for surveillance Repealed
  6. A.1Objectives Repealed
  7. General requirements and criteria Repealed
  8. 1Division 1 Repealed
  9. 2Division 2 Repealed
  10. 3Division 3 Repealed
  11. 4Division 4 Repealed
  12. 5Division 5 Repealed
  13. 6Division 6 Repealed
  14. BSurveillance for avian influenza in poultry Repealed
  15. 1Division 1 Repealed
  16. 2Division 2 Repealed
  17. 3Division 3 Repealed
  18. 4Sampling shall be stratified throughout the territory of the whole Member State, so that samples can be considered as representative for the whole of the Member State, taking into account: Repealed
  19. 5Based on a risk assessment and the specific situation in the Member State concerned, the sampling design shall also consider: Repealed
  20. Specific requirements for detection of infections with H5/H7 subtypes of avian influenza in ducks, geese and quail Repealed
  21. 1Division 1 Repealed
  22. 2Division 2 Repealed
  23. 3Division 3 Repealed
  24. Laboratory testing Repealed
  25. 1Division 1 Repealed
  26. 2Division 2 Repealed
  27. 3All positive serological findings shall be confirmed by the NL by a haemagglutination-inhibition test, using designated strains supplied by the CRL: Repealed
  28. Annex II: Guidelines on the implementation of surveillance programmes for avian influenza in wild birds to be carried out in the Member States Repealed
  29. Objectives, general requirements and criteria for surveillance Repealed
  30. A1Objectives Repealed
  31. General requirements and criteria Repealed
  32. 1Division 1 Repealed
  33. 2Division 2 Repealed
  34. 3Division 3 Repealed
  35. 4Division 4 Repealed
  36. Surveillance for avian influenza in wild birds Repealed
  37. Design and implementation Repealed
  38. Sampling procedures Repealed
  39. 1Division 1 Repealed
  40. 2Division 2 Repealed
  41. 3Division 3 Repealed
  42. 4Division 4 Repealed
  43. Laboratory testing Repealed
  44. 1Division 1 Repealed
  45. 2Division 2 Repealed
  46. 3Division 3 Repealed
  47. 4Division 4 Repealed
  48. 5Division 5 Repealed
  49. DDivision D Repealed
  50. EDivision E Repealed
  51. Annex IIIAnnex III Repealed

1Approval of surveillance programmes for avian influenzaF1

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2Amendments to Decision 2004/450/ECF1

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A.1ObjectivesF1

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BSurveillance for avian influenza in poultryF1

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4Sampling shall be stratified throughout the territory of the whole Member State, so that samples can be considered as representative for the whole of the Member State, taking into account:F1

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5Based on a risk assessment and the specific situation in the Member State concerned, the sampling design shall also consider:F1

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3All positive serological findings shall be confirmed by the NL by a haemagglutination-inhibition test, using designated strains supplied by the CRL:F1

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A1ObjectivesF1

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Design and implementation

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Annex IIIF1

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